Canonical Allele Identifier: CA474822946
Gene: OR5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.59211106C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.59443633C>A , CM000673.2:g.59443633C>A GRCh38
NC_000011.9:g.59211106C>A , CM000673.1:g.59211106C>A GRCh37
NC_000011.8:g.58967682C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641045.1:c.465C>A MANE Select ENSP00000493195.1:p.Gly155=
ENST00000302030.2:c.465C>A ENSP00000303096.2:p.Gly155=
NM_001004728.1:c.465C>A NP_001004728.1:p.Gly155=
XM_011544810.1:c.465C>A XP_011543112.1:p.Gly155=
NM_001004728.2:c.465C>A MANE Select NP_001004728.1:p.Gly155=
Search 100 bp 5'
Search 100 bp 3'